Canonical Allele Identifier: CA2726126112
Gene: NAB2 HGNC NCBI

Linked Data

dbSNP Id: rs2033292273

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.57094443A>T , CM000674.2:g.57094443A>T GRCh38
NC_000012.11:g.57488226A>T , CM000674.1:g.57488226A>T GRCh37
NC_000012.10:g.55774493A>T NCBI36
NG_021272.1:g.21971T>A
NG_021272.2:g.42697T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000300131.8:c.1469-169A>T MANE Select ENSP00000300131.3:n.1469-169A>T
ENST00000300131.7:c.1469-169A>T ENSP00000300131.3:n.1469-169A>T
ENST00000342556.6:c.1277-169A>T ENSP00000341491.6:n.1277-169A>T
NM_005967.3:c.1469-169A>T NP_005958.1:n.1469-169A>T
XM_005268894.2:c.1277-169A>T XP_005268951.1:n.1277-169A>T
NM_001330305.1:c.1277-169A>T NP_001317234.1:n.1277-169A>T
NM_005967.4:c.1469-169A>T MANE Select NP_005958.1:n.1469-169A>T
NM_001330305.2:c.1277-169A>T NP_001317234.1:n.1277-169A>T